FDA Drug Recalls

3 recalls · Class I, newest first

Apr 21, 2017 Class I · High risk

Presence of Particulate Matter: human hair found within an internal sample syringe.

Ongoing Particulate / foreign matter Hospira Inc. NDC 0409-1775-10 D-0862-2017

Mar 12, 2017 Class I · High risk

Defective Delivery System; reports of the device failing to activate which could result in a patient not receiving medication

Ongoing Packaging defect Meridian Medical Technologies a Pfizer Company NDC 49502-500-02 D-0691-2017

Mar 12, 2017 Class I · High risk

Defective Delivery System; reports of the device failing to activate which could result in a patient not receiving medication

Ongoing Packaging defect Meridian Medical Technologies a Pfizer Company NDC 49502-500-02 D-0690-2017

Recalls by year